Have questions? Visit https://www.reddit.com/r/SNPedia

rs587777241

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587777241(C;C)
Make rs587777241(C;G)
ReferenceGRCh38 38.1/142
Chromosome22
Position17207277
GeneCECR1
is asnp
is mentioned by
dbSNPrs587777241
ebirs587777241
HLIrs587777241
Exacrs587777241
Varsomers587777241
Maprs587777241
PheGenIrs587777241
hapmaprs587777241
1000 genomesrs587777241
hgdprs587777241
ensemblrs587777241
gopubmedrs587777241
geneviewrs587777241
scholarrs587777241
googlers587777241
pharmgkbrs587777241
gwascentralrs587777241
openSNPrs587777241
23andMers587777241
23andMe allrs587777241
SNP Nexus

SNPshotrs587777241
SNPdbers587777241
MSV3drs587777241
GWAS Ctlgrs587777241
Max Magnitude0
ClinVar
Risk rs587777241(C;C)
Alt rs587777241(C;C)
Reference rs587777241(G;G)
Significance Pathogenic
Disease Polyarteritis nodosa
Variation info
Gene CECR1
CLNDBN Polyarteritis nodosa
Reversed 0
HGVS NC_000022.10:g.17688167G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000106383.3,